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Human basal cell carcinoma: the induction of anagen hair follicle differentiation.

人基底细胞癌: 诱导毛囊分化。

  • 影响因子:1.09
  • DOI:10.1111/ced.14108
  • 作者列表:"Morgan HJ","Benketah A","Olivero C","Rees E","Ziaj S","Mukhtar A","Lanfredini S","Patel GK
  • 发表时间:2020-04-01
Abstract

BACKGROUND:Consistent with cancer stem cell driven pattern of growth, human basal cell carcinomas (BCCs) demonstrate differentiation along hair follicle (HF) lineages. AIM:To define the pattern of differentiation and therapeutic targets that promote BCC differentiation and therefore BCC cancer stem cell exhaustion. METHODS:An alkaline phosphatase substrate kit was used to determine dermal papilla cells within the BCC stroma. Autonomous HF cycle-dependent gene expression was identified by analysis of the human homologues of a murine gene set (total 2289 genes) that is differentially expressed in hair cycle phases. The findings were validated by quantitative real-time PCR and immunofluorescence, as well as in vitro transforming growth factor (TGF)-β2 stimulation of BCC cancer stem cell colonies. RESULTS:As in the HF, keratin expression in the inner root sheath and matrix in BCC correlated with proliferative index and was tightly regulated, despite the absence of dermal papilla cells. Cross-species microarray analysis comparing human BCC and murine synchronous HF growth cycle datasets revealed 74% concordance with telogen differentiation compared with anagen (23%, P < 0.01) and catagen (49%; P < 0.01). Incomplete anagen differentiation within BCC was characterized by reduced expression of the anagen master regulator DLX3 (-5.5-fold), and increased expression of telogen-associated genes: AEBP1 (2.2-fold), DEFB8 (35.3-fold), MMP3 (106.0-fold) and MMP12 (12.9-fold). Restoration of dermal papilla signals by in vitro addition of TGF-β2 enhanced anagen differentiation. CONCLUSION:Our findings show that BCC cells differentiate along HF lineages and may be susceptible to exogenous HF cycle modulators.

摘要

背景: 与肿瘤干细胞驱动的生长模式一致,人基底细胞癌 (BCCs) 显示沿毛囊 (HF) 谱系分化。 目的: 确定促进BCC分化从而BCC癌干细胞衰竭的分化模式和治疗靶点。 方法: 采用碱性磷酸酶底物试剂盒测定BCC基质内的毛乳头细胞。通过分析在毛发周期阶段差异表达的鼠基因集 (共 2289 个基因) 的人类同系物,鉴定自主HF周期依赖性基因表达。通过定量实时PCR和免疫荧光,以及体外转化生长因子 (TGF)-β 2 刺激BCC肿瘤干细胞集落来验证这些发现。 结果: 与HF一样,尽管没有毛乳头细胞,但BCC内根鞘和基质中角蛋白的表达与增殖指数相关,并受到严格调控。比较人BCC和鼠同步HF生长周期数据集的跨物种微阵列分析显示,与anagen (74%,P <23%) 和catagen (0.01) 相比,与休止期分化的一致性为 49%; P <0.01)。BCC内的不完全anagen分化的特征是anagen主调控因子DLX3 的表达减少 (-5.5 倍),并且休止期相关基因的表达增加: AEBP1 (2.2 倍),DEFB8 (35.3 倍) 、MMP3 (106.0 倍) 和MMP12 (12.9 倍)。通过体外添加tgf-β 2 增强anagen分化恢复毛乳头信号。 结论: 我们的研究结果表明,BCC细胞沿HF谱系分化,可能对外源性HF周期调节剂敏感。

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影响因子:0.96
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皮肤肿瘤方向

皮肤肿瘤是发生在皮肤的细胞增生性疾病,是一种常见病。发生于皮内或皮下组织的新生物,种类很多,临床上分良性肿瘤和恶性肿瘤。恶性肿瘤可以不断增殖,引起转移,威胁生命,称为皮肤癌。

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